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GRAVISET Varioline, ENFit - Indonesia BPOM Medical Device Registration

GRAVISET Varioline, ENFit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902024168. The device is manufactured by FRESENIUS KABI (NANCHANG) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRESENIUS KABI INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
GRAVISET Varioline, ENFit
Analysis ID: AKL 20902024168

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FRESENIUS KABI INDONESIA

AR Address

Menara Bidakara 1 Lt 19, Jl. Jend Gatot Subroto Kav 71-73

Registration Date

Feb 13, 2024

Expiry Date

Oct 19, 2028

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set

Non Electromedic Sterile

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